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Plasma phosphorylated TDP-43 levels are elevated in patients with frontotemporal dementia carrying a C9orf72 repeat expansion or a GRN mutation

Journal of neurology, neurosurgery and psychiatry, 2014-06, Vol.85 (6), p.684-691

2014

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HSP70-2 (HSPA1B) is Associated with Noncognitive Symptoms in Late-Onset Alzheimer's Disease

Journal of geriatric psychiatry and neurology, 2003-09, Vol.16 (3), p.146-150

2003

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Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study

Neurobiology of aging, 2015-05, Vol.36 (5), p.2005.e15-2005.e22

2015

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Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort

Human mutation, 2015-12, Vol.36 (12), p.1226-1235

2015

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Association of biological sex with clinical outcomes and biomarkers of Alzheimer’s disease in adults with Down syndrome

Brain communications, 2023, Vol.5 (2), p.fcad074-fcad074

2023

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Torsin A haplotype predisposes to idiopathic dystonia

Annals of neurology, 2005-05, Vol.57 (5), p.765-767

2005

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Mild cholesterol depletion reduces amyloid-β production by impairing APP trafficking to the cell surface

Journal of neurochemistry, 2009-07, Vol.110 (1), p.220-230

2009

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S.O.4 - A POGLUT1 mutation causes a muscular dystrophy with reduced notch signaling and satellite cell loss

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S90-S90

2016

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Tyrosinase exacerbates dopamine toxicity but is not genetically associated with Parkinson's disease

Journal of neurochemistry, 2005-04, Vol.93 (1), p.246-256

2005

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Trading Genes along the Silk Road: mtDNA Sequences and the Origin of Central Asian Populations

American journal of human genetics, 1998-12, Vol.63 (6), p.1824-1838

1998

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Use of plasma biomarkers for AT(N) classification of neurodegenerative dementias

Journal of neurology, neurosurgery and psychiatry, 2021-11, Vol.92 (11), p.1206

2021

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Conflicting Results Regarding the Semaphorin Gene ( SEMA5A) and the Risk for Parkinson Disease

American journal of human genetics, 2006-06, Vol.78 (6), p.1082-1083

2006

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Genetic structure of north-west Africa revealed by STR analysis

European journal of human genetics : EJHG, 2000-05, Vol.8 (5), p.360-366

2000

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Clinical, Neuropathologic, and Biochemical Profile of the Amyloid Precursor Protein I716F Mutation

Journal of neuropathology and experimental neurology, 2010-01, Vol.69 (1), p.53-59

2010

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Dystonia and the Nuclear Envelope

Neuron (Cambridge, Mass.), 2005-12, Vol.48 (6), p.875-877

2005

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Homocysteine and cognitive impairment. Relation with diagnosis and neuropsychological performance

Dementia and geriatric cognitive disorders, 2008-01, Vol.26 (6), p.506

2008

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Clinical and neuroimaging features of familial C9FTD/ALS: A case report

Journal of the neurological sciences, 2013-10, Vol.333, p.e446-e447

2013

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Sex-Specific Migration Patterns in Central Asian Populations, Revealed by Analysis of Y-Chromosome Short Tandem Repeats and mtDNA

American journal of human genetics, 1999-07, Vol.65 (1), p.208-219

1999

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Lack of association between CX3CR1 V249I and T280M polymorphisms and risk of Parkinson's disease in a Greek population

Genetic testing and molecular biomarkers, 2012-08, Vol.16 (8), p.974

2012

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Paraoxonase 1 ( PON1) gene polymorphisms and Parkinson’s disease in a Finnish population

Neuroscience letters, 2004-09, Vol.367 (2), p.168-170

2004

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Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

Nature communications, 2021-06, Vol.12 (1), p.3417-16, Article 3417

2021

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Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: Evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease

Neuroscience letters, 2005-07, Vol.382 (1), p.191-194

2005

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Possible increased risk for Alzheimer's disease associated with neprilysin gene

Journal of Neural Transmission, 2003-06, Vol.110 (6), p.651-657

2003

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Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients

BMC neurology, 2005-06, Vol.5 (1), p.11-11, Article 11

2005

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Assessment of PINK1 ( PARK6) polymorphisms in Finnish PD

Neurobiology of aging, 2006-06, Vol.27 (6), p.906-907

2006

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Plasma phosphorylated TDP-43 levels are elevated in patients with frontotemporal dementia carrying a C9orf72 repeat expansion or a GRN mutation

HSP70-2 (HSPA1B) is Associated with Noncognitive Symptoms in Late-Onset Alzheimer's Disease

Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study

Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort

Association of biological sex with clinical outcomes and biomarkers of Alzheimer’s disease in adults with Down syndrome

Torsin A haplotype predisposes to idiopathic dystonia

Mild cholesterol depletion reduces amyloid-β production by impairing APP trafficking to the cell surface

S.O.4 - A POGLUT1 mutation causes a muscular dystrophy with reduced notch signaling and satellite cell loss

Tyrosinase exacerbates dopamine toxicity but is not genetically associated with Parkinson's disease

Trading Genes along the Silk Road: mtDNA Sequences and the Origin of Central Asian Populations

Use of plasma biomarkers for AT(N) classification of neurodegenerative dementias

Conflicting Results Regarding the Semaphorin Gene ( SEMA5A) and the Risk for Parkinson Disease

Genetic structure of north-west Africa revealed by STR analysis

Clinical, Neuropathologic, and Biochemical Profile of the Amyloid Precursor Protein I716F Mutation

Dystonia and the Nuclear Envelope

Homocysteine and cognitive impairment. Relation with diagnosis and neuropsychological performance

Clinical and neuroimaging features of familial C9FTD/ALS: A case report

Sex-Specific Migration Patterns in Central Asian Populations, Revealed by Analysis of Y-Chromosome Short Tandem Repeats and mtDNA

Lack of association between CX3CR1 V249I and T280M polymorphisms and risk of Parkinson's disease in a Greek population

Paraoxonase 1 ( PON1) gene polymorphisms and Parkinson’s disease in a Finnish population

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: Evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease

Possible increased risk for Alzheimer's disease associated with neprilysin gene

Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients

Assessment of PINK1 ( PARK6) polymorphisms in Finnish PD

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